Daigaku Yasukazu, Keszthelyi Andrea, Müller Carolin A, Miyabe Izumi, Brooks Tony, Retkute Renata, Hubank Mike, Nieduszynski Conrad A, Carr Antony M
Genome Damage and Stability Centre, University of Sussex, Brighton, UK.
Sir William Dunn School of Pathology, University of Oxford, Oxford, UK.
Nat Struct Mol Biol. 2015 Mar;22(3):192-198. doi: 10.1038/nsmb.2962. Epub 2015 Feb 9.
Three eukaryotic DNA polymerases are essential for genome replication. Polymerase (Pol) α-primase initiates each synthesis event and is rapidly replaced by processive DNA polymerases: Polɛ replicates the leading strand, whereas Polδ performs lagging-strand synthesis. However, it is not known whether this division of labor is maintained across the whole genome or how uniform it is within single replicons. Using Schizosaccharomyces pombe, we have developed a polymerase usage sequencing (Pu-seq) strategy to map polymerase usage genome wide. Pu-seq provides direct replication-origin location and efficiency data and indirect estimates of replication timing. We confirm that the division of labor is broadly maintained across an entire genome. However, our data suggest a subtle variability in the usage of the two polymerases within individual replicons. We propose that this results from occasional leading-strand initiation by Polδ followed by exchange for Polɛ.
三种真核生物DNA聚合酶对基因组复制至关重要。聚合酶(Pol)α-引发酶启动每个合成事件,并迅速被持续性DNA聚合酶取代:Polɛ复制前导链,而Polδ进行滞后链合成。然而,尚不清楚这种分工是否在整个基因组中得以维持,或者在单个复制子内的一致性如何。利用粟酒裂殖酵母,我们开发了一种聚合酶使用测序(Pu-seq)策略,以在全基因组范围内绘制聚合酶的使用情况。Pu-seq提供直接的复制起点位置和效率数据以及复制时间的间接估计。我们证实这种分工在整个基因组中大致得以维持。然而,我们的数据表明,在单个复制子内两种聚合酶的使用存在细微差异。我们认为这是由于Polδ偶尔引发前导链,随后替换为Polɛ所致。